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The vegetatively propagated `Fire Kiss' clone of the hybrid Zygopetalum Redvale orchid has appealing potted-plant characteristics, including fragrant flowers that are waxy lime-green and dark maroon with a broad, three-lobed, magenta and white labellum. We performed experiments to quantify how temperature influenced leaf unfolding and expansion, time from visible inflorescence to flower, and longevity of individual flowers and inflorescences. Plants were grown in controlled-environment chambers with constant temperature set points of 14, 17, 20, 23, 26, and 29 °C and an irradiance of 150 μmol·m^-2·s^-1 for 9 h·d^-1. As actual temperature increased from 14 to 25 °C, the time to produce one leaf decreased from 46 to 19 days. Individual plants were also transferred from a greenhouse to the chambers on the date that an inflorescence was first visible or the first flower of an inflorescence opened. Time from visible inflorescence to open flower decreased from 73 days at 14 °C to 30 days at 26 °C. As temperature increased from 14 to 29 °C, flower and inflorescence longevity decreased from 37 and 38 days to 13 and 15 days, respectively. Data were converted to rates, and thermal time models were developed to predict time to flower and senescence at different temperatures. The base temperature was estimated at 6.2 °C for leaf unfolding, 3.5 °C for time to flower, and 3.7 °C for flower longevity. These models could be used by greenhouse growers to more accurately schedule Zygopetalum flowering crops for particular market dates.

Heating accounts for up to 30% of total operating costs for greenhouse operations in northern latitudes. Growers often lower air temperatures for production to reduce energy costs; however, this causes delays in development even in cold-tolerant crops, such as petunia (Petunia ×hybrida). This delay increases production time and can reduce profitability. Recent studies on low air temperature bedding plant production indicate petunia as a strong potential candidate for using lower air temperatures in combination with bench-top root-zone heating (RZH) to avoid or reduce delays in development. The objectives of this study were to 1) quantify time to flower (TTF) of seven petunia cultivars and two recombinant inbred lines (RILs) when the mean daily air temperature (MDT) was lowered by 5 °C and bench-top RZH was used and 2) determine if a high-quality petunia crop can be produced on RZH. Petunia ‘Sun Spun Burgundy’, ‘Sun Spun Lavender Star’, ‘Sanguna Patio Red’, ‘Potunia Plus Red’, ‘Potunia Plus Purple’, ‘Supertunia Red’, ‘Supertunia Bordeaux’, and two RILs, IA160 and IA349, were grown in a greenhouse with an MDT of 15 °C without RZH or with a RZH set point of 21, 24, or 27 °C. Additionally, a commercial control (CC) was established by growing plants without RZH at an MDT of 20 °C. All plants were grown under a 16-hour photoperiod to provide a daily light integral (DLI) of ≈12 mol·m⁻²·d⁻¹. Time to flower was shorter at higher RZH set points. For example, TTF of ‘Potunia Plus Red’ was 56, 52, 49, or 47 days for plants grown at an MDT of 15 °C without RZH, or with RZH set points of 21, 24, or 27 °C, respectively. When a RZH set point of 27 °C was employed, TTF of all cultivars and inbred lines, except ‘Potunia Plus Red’ and ‘Sanguna Patio Red’, was similar to plants grown in the CC. Shorter stem length, lower growth index, and smaller shoot dry mass (SDM) at flowering were observed for plants grown under lower air temperatures with RZH, resulting in a more compact and high-quality plant. Producing a compact plant in a shorter time period is beneficial for growers; thus, results suggest that MDT can be lowered to 15 °C for petunia production when a RZH set point of 27 °C is employed.

In 2003, commercial greenhouse growers in the United States imported 724 million nonrooted cuttings valued at $53 million. During transit and storage, cuttings can be exposed to environmental stresses (e.g., low or high temperature), which can consequently decrease quality, rooting, and subsequent plant performance. We performed experiments to quantify how temperature and storage duration of cuttings influence root initiation, root number, lateral branch count and length, and time to flower of Tiny Tunia `Violet Ice' petunia (Petunia × hybrida hort. Vilm. -Andr.). Dry or wet cuttings were harvested and packaged into perforated bags within small, ventilated boxes and then into traditional shipping boxes. The boxes were placed in environmental chambers with temperature setpoints of 0, 5, 10, 15, 20, 25, or 30 °C for 0, 1, 2, 3, 4, or 5 d. Cuttings were then rooted in a propagation house at 26 °C with a vapor pressure deficit of 0.3 kPa under ambient photo-periods. The visual quality rating of dry packaged cuttings decreased with increasing temperature and shipping duration. After 2 d at ≥25 °C, cuttings were horticulturally unacceptable due to water stress and chlorophyll degradation and they never fully recovered. Dry- or wet-packaged cuttings held at temperatures of 0 to 30 °C formed significantly fewer roots and lateral branches as duration increased from 1–5 d. Although cuttings held for 5 d at 0 °C produced 60% fewer lateral branches, they subsequently flowered 5 d earlier than plants held at 0 °C for 1 d. Therefore, exposure to temperatures >15 °C for ≥3 d can reduce petunia cutting quality, delay rooting, and decrease plant size at flowering.

Miltoniopsis orchids have appealing potted-plant characteristics, including large, fragrant, and showy pansylike flowers that range from white and yellow to shades of red and purple. Scheduling orchid hybrids to flower on specific dates requires knowledge of how light and temperature regulate the flowering process. We performed experiments to determine whether a 9- or 16-h photoperiod [short day (SD) or long day (LD)] before vernalization and vernalization temperatures of 8, 11, 14, 17, 20, or 23 °C under SD or LD regulate flowering of potted Miltoniopsis orchids. Flowering of Miltoniopsis Augres `Trinity' was promoted most when plants were exposed to SD and then vernalized at 11 or 14 °C. Additional experiments were performed to determine how durations of prevernalization SD and vernalization at 14 °C influenced flowering of Miltoniopsis Augres `Trinity' and Eastern Bay `Russian'. Plants were placed under SD or LD at 20 °C for 0, 4, 8, 12, or 16 weeks and then transferred to 14 °C under SD for 8 weeks. Another set of plants was placed under SD or LD at 20 °C for 8 weeks and then transferred to 14 °C with SD for 0, 3, 6, 9, or 12 weeks. After treatments, plants were grown in a common environment at 20 °C with LD. Flowering of Miltoniopsis Augres `Trinity' was most complete and uniform (≥90%) when plants were exposed to SD for 4 or 8 weeks before 8 weeks of vernalization at 14 °C. Flowering percentage of Miltoniopsis Eastern Bay `Russian' was ≥80 regardless of prevernalization photoperiod or duration. This information could be used by greenhouse growers and orchid hobbyists to more reliably induce flowering of potted Miltoniopsis orchids.

A majority of commercial propagation of herbaceous ornamental cuttings occurs during the winter when the photosynthetic daily light integral (DLI) is relatively low. We quantified how the mean DLI influenced rooting and subsequent growth and development of two popular vegetatively propagated species, New Guinea impatiens (Impatiens hawkeri Bull.) and petunia (Petunia ×hybrida hort. Vilm.-Andr.). Three cultivars of each species were propagated under a mean DLI ranging from 1.2 to 10.7 mol·m⁻²·d⁻¹. Cuttings were rooted in a controlled greenhouse environment maintained at 24 to 25 °C with overhead mist, a vapor-pressure deficit of 0.3 kPa, and a 12-h photoperiod. Rooting and growth evaluations of cuttings were made after 8 to 16 d. In a separate experiment, rooted cuttings under DLI treatments were then transplanted into 10-cm containers and grown in a common greenhouse at 21 ± 2 °C under a 16-h photoperiod to identify any residual effects on subsequent growth and development. In both species, rooting, biomass accumulation, and quality of cuttings increased and subsequent time to flower generally decreased as mean propagation DLI increased. For example, root number of petunia ‘Tiny Tunia Violet Ice’ after 16 days of propagation increased from 17 to 40 as the propagation DLI increased from 1.2 to 7.5 mol·m⁻²·d⁻¹. In addition, cutting shoot height decreased from 6.3 to 4.5 cm, and root and shoot dry biomass of cuttings harvested after 16 days of propagation increased by 737% and 106%, respectively. Subsequent time to flower for ‘Tiny Tunia Violet Ice’ from the beginning of propagation decreased from 50 to 29 days as propagation DLI increased from 1.4 to 10.7 mol·m⁻²·d⁻¹ regardless of the DLI provided after propagation. In New Guinea impatiens ‘Harmony White’, root and shoot dry weight of cuttings increased by 1038% and 82%, respectively, and subsequent time to flower decreased from 85 to 70 days as the propagation DLI increased from 1.2 to 10.7 mol·m⁻²·d⁻¹. These experiments quantify the role of the photosynthetic DLI during propagation on the rooting and subsequent growth and development of vegetatively propagated herbaceous ornamental cuttings.

Crown division, tissue culture, and culm cuttings are methods for propagating purple fountain grass [Pennisetum ×advena Wipff and Veldkamp (formerly known as Pennisetum setaceum Forsk. Chiov. ‘Rubrum’)]. However, propagation by culm cuttings is becoming an economically attractive method for quick liner production. Our objective was to quantify the impact of propagation daily light integral (PDLI) and root-zone temperature (RZT) on root and culm development of single-internode purple fountain grass culm cuttings. Before insertion into the rooting substrate, cuttings were treated with a basal rooting hormone solution containing 1000 mg·L⁻¹ indole-3-butyric acid (IBA) + 500 mg·L⁻¹ 1-naphthaleneacetic acid (NAA). The cuttings were placed in a glass-glazed greenhouse with an air temperature of 23 °C and benches with RZT set points of 21, 23, 25, or 27 °C. PDLIs of 4 and 10 mol·m⁻²·d⁻¹ (Expt. 1) or 8 and 16 mol·m⁻²·d⁻¹ (Expt. 2) were provided. After 28 d, culm and root densities (number) increased as the RZT increased from 21 to 27 °C, regardless of PDLI during Expt. 1. Compared with 4 mol·m⁻²·d⁻¹, a PDLI of 10 mol·m⁻²·d⁻¹ generally resulted in the greatest root biomass accumulation. For example, as PDLI increased from 4 to 10 mol·m⁻²·d⁻¹, root dry mass increased by 105%, 152%, and 183% at RZTs of 21, 25, and 27 °C, respectively. In Expt. 2, as the RZT increased from 21 to 23 °C, root dry mass increased by 70% under a PDLI of 8 mol·m⁻²·d⁻¹. However, root dry mass was similar among all RZTs under a PDLI of 16 mol·m⁻²·d⁻¹. Our results indicate that single-internode culm cuttings of purple fountain grass can be most efficiently propagated under PDLIs of 8–10 mol·m⁻²·d⁻¹ together with RZT set points of 23 to 25 °C for quick liner production.

The plant growth regulator (PGR) ethephon [(2-chloroethyl) phosphonic acid; ETH] can be sprayed on floriculture crops to inhibit internode elongation, hinder apical dominance, increase lateral branching, and abort flower buds and flowers. However, the efficacy of ETH can be reduced as the pH of the carrier water used to mix the spray solution or temperature increase. Therefore, our objective was to quantify how the efficacy of ethephon sprays is influenced by carrier water alkalinity (CaCO₃; ALK) and the air temperature at application (TEMP). Young plants of verbena (Verbena peruviana) ‘Aztec Blue Velvet’, ivy geranium (Pelargonium ×peltatum) ‘Precision Pink’, and petunia (Petunia ×hybrida) ‘Easy Wave Neon Rose’ were transplanted into 11-cm-diameter containers and grown in a greenhouse with an average daily air temperature (ADT) set point of 21 °C. Before the ETH spray application(s), the ADT in each greenhouse compartment was changed from a set point of 21 °C to 14, 17, 20, 23, or 26 °C for ≈24 hours. Plants were sprayed with 0, 250, 500, or 750 mg·L⁻¹ ETH mixed with carrier water containing ≈50, 150, or 300 mg·L⁻¹ CaCO₃ 2 and 3 weeks (Expt. 1) or 1 or 2 weeks (Expt. 2) after transplant. Generally, high ALK had a negative effect on spray efficacy. For example, an increase in ALK from 50 to 300 mg·L⁻¹ CaCO₃ resulted in one and five fewer ivy geranium and verbena branches, respectively. In addition, as application TEMP increased above 23 °C, chemical efficacy generally decreased in all species. For instance, as ETH increased from 0 to 750 mg·L⁻¹ across ALKs, inflorescence number of ivy geraniums increased from 7 to 18 at a TEMP of 23 °C, but was unaffected at 26 °C. Based on our results, we can conclude that both ALK and TEMP influence ETH efficacy and are additional factors for greenhouse growers to consider when making applications.

Domestic production of culinary herbs continues to increase in the United States. Culinary herbs are primarily propagated by seed; however, some herbs have poor germination rates and slow growth. Thus, there are advantages of propagating herbs by vegetative stem-tip cuttings as they lead to true-to-type plants and a shortened production time. Previous research of ornamental young plants and finished culinary herbs have shown a reduction in rooting time and increases in plant quality with increases in the photosynthetic daily light integral (DLI). To our knowledge, little to no research has addressed how the DLI influences culinary herb liner quality. Therefore, the objectives of this study were to quantify morphological traits of five economically important culinary herbs when grown under DLIs ranging from 2.8 to 16.4 mol·m⁻²·d⁻¹. Stem-tip cuttings of Greek oregano (Origanum vulgare var. hirtum), rosemary ‘Arp’ (Rosmarinus officinalis), sage ‘Extrakta’ (Salvia officinalis), spearmint ‘Spanish’ (Mentha spicata), and thyme ‘German Winter’ (Thymus vulgaris) were excised from stock plants and rooted under no shade or aluminum shading of 36%, 56%, or 76% to create a range of DLI treatments. After 9 days (spearmint) or 16 days (all other genera) of DLI treatments, the root, shoot, and total dry mass of all culinary herb liners generally increased by 105% to 449%, 52% to 142%, and 82% to 170%, respectively, as the DLI increased from 2.8 to 16.4 mol·m⁻²·d⁻¹ or genus-specific DLI optimums. Stem length of oregano, spearmint, and thyme decreased by 37%, 28%, and 27%, respectively, as the DLI increased from 2.8 to 16.4 mol·m⁻²·d⁻¹. However, stem length of rosemary and sage were unaffected by the DLI. The quality index of all genera was greatest at DLIs from 10.4 to 16.4 mol·m⁻²·d⁻¹. Furthermore, all culinary herbs grown under a DLI of ≤6 mol·m⁻²·d⁻¹ had low root and shoot dry mass accumulation; and oregano, spearmint, and thyme were generally taller. Therefore, DLIs between 10 to 12 mol·m⁻²·d⁻¹ should be maintained during culinary herb propagation, because a DLI ≥16 mol·m⁻²·d⁻¹ may be deleterious and energy inefficient if supplemental lighting use is increased.

Annual bedding plant seedlings or plugs are considered high quality when they are compact, fully rooted transplants with a large stem caliper and high root dry mass. Greenhouses in northern latitudes rely on supplemental lighting (SL) from high-pressure sodium lamps (HPS) during winter months to achieve high-quality, finished plugs. Light-emitting diodes (LEDs) offer higher energy efficiencies, a long operating life, and precise waveband specificity that can eliminate wavebands not considered useful. Seedlings of Antirrhinum, Catharanthus, Celosia, Impatiens, Pelargonium, Petunia, Tagetes, Salvia, and Viola were grown at 21 °C under a 16-hour photoperiod of ambient solar light and SL of 100 μmol·m⁻²·s^–1 from either HPS lamps or LED arrays with varying proportions (%) of red:blue light (100:0, 85:15, or 70:30). Height of Catharanthus, Celosia, Impatiens, Petunia, Tagetes, Salvia, and Viola was 31%, 29%, 31%, 55%, 20%, 9%, and 35% shorter, respectively, for seedlings grown under the 85:15 red:blue LEDs compared with those grown under HPS lamps. Additionally, stem caliper of Antirrhinum, Pelargonium, and Tagetes was 16%, 8%, and 13% larger, respectively, for seedlings grown under the 85:15 red:blue LEDs compared with seedlings grown under HPS lamps. The quality index (QI), a quantitative measurement of quality, was similar for Antirrhinum, Catharanthus, Impatiens, Pelargonium, and Tagetes grown under LEDs and HPS lamps. However, it was significantly higher for Petunia, Salvia, and Viola under 85:15, 70:30, and 100:0 red:blue LEDs than under HPS lamps, respectively. These results indicate that seedling quality for the majority of the species tested under SL from LEDs providing both red and blue light was similar or higher than those grown under HPS lamps.

Flowering potted orchids has become one of the largest segments of floriculture worldwide. Large-scale production of cuts or potted plants exists in China, Germany, Japan, The Netherlands, Taiwan, Thailand, and the United States. Despite the value of orchids, the flowering physiology of most orchid genera is not well described. Therefore, scheduling flowering crops for specific market dates (such as Easter or Mother's Day) is not possible for most genera. This paper summarizes world orchid production and reviews how environmental factors regulate growth and flowering of several commercially important orchid genera: Cattleya, Cymbidium, Dendrobium, Miltoniopsis, Phalaenopsis, and Zygopetalum. These genera primarily flower in response to relatively low temperatures, and, for some species and hybrids, flowering is promoted when the plants are also exposed to short photoperiods. Effects of light and temperature on growth and development are summarized for these genera, and implications for controlled production are discussed.